The role of PPARα in lipid metabolism and obesity: Focusing on the effects of estrogen on PPARα actions

被引:252
作者
Yoon, Michung [1 ]
机构
[1] Mokwon Univ, Dept Life Sci, Taejon 302729, South Korea
关键词
PPAR alpha; Obesity; Lipid metabolism; Estrogen; PROLIFERATOR-ACTIVATED-RECEPTOR; FATTY-ACID OXIDATION; RETINOID-X-RECEPTOR; PALMITOYLTRANSFERASE-I GENE; HUMAN UNCOUPLING PROTEIN-3; MESSENGER-RNA LEVELS; ORPHAN NUCLEAR RECEPTORS; HIGH-DENSITY-LIPOPROTEIN; DIET-INDUCED OBESITY; APOLIPOPROTEIN-A-I;
D O I
10.1016/j.phrs.2009.02.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Peroxisome proliferator-activated receptor a (PPAR alpha) is a ligand-activated transcription factor that belongs to the steroid hormone receptor superfamily. PPAR alpha is expressed predominantly in tissues that have a high level of fatty acid catabolism, such as liver, heart, and muscle. PPAR alpha regulates the expression of a number of genes critical for lipid and lipoprotein metabolism. PPAR alpha ligand fibrates have been used for the treatment of dyslipidemia due to their ability to lower plasma triglyceride levels and elevate HDL cholesterol levels. PPAR alpha activators have been shown to regulate obesity in rodents by both increasing hepatic fatty acid oxidation and decreasing the levels of circulating triglycerides responsible for adipose cell hypertrophy and hyperplasia. However, these effects of PPAR alpha on obesity and lipid metabolism may be exerted with sexual dimorphism and seem to be influenced by estrogen. Estrogen inhibits the actions of PPAR alpha on obesity and lipid metabolism through its effects on PPAR alpha-dependent regulation of target genes. Thus, the use of fibrates seems to be effective in men and postmenopausal women with obesity and lipid disorders, but not in premenopausal women with functioning ovaries. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:151 / 159
页数:9
相关论文
共 157 条
  • [51] Orphan nuclear receptors:: From gene to function
    Giguère, V
    [J]. ENDOCRINE REVIEWS, 1999, 20 (05) : 689 - 725
  • [52] COMPARISON OF THE EFFECTS OF LOVASTATIN AND GEMFIBROZIL ON LIPIDS AND GLUCOSE CONTROL IN NON-INSULIN-DEPENDENT DIABETES-MELLITUS
    GOLDBERG, R
    LABELLE, P
    ZUPKIS, R
    RONCA, P
    [J]. AMERICAN JOURNAL OF CARDIOLOGY, 1990, 66 (08) : B16 - B21
  • [53] Mechanism of action of the nongenotoxic peroxisome proliferators:: Role of che peroxisome proliferator-activated receptor α
    Gonzalez, FJ
    Peters, JM
    Cattley, RC
    [J]. JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1998, 90 (22) : 1702 - 1709
  • [54] NUCLEAR RECEPTORS ENHANCE OUR UNDERSTANDING OF TRANSCRIPTION REGULATION
    GREEN, S
    CHAMBON, P
    [J]. TRENDS IN GENETICS, 1988, 4 (11) : 309 - 314
  • [55] Peroxisome proliferator-activated receptor α activators improve insulin sensitivity and reduce adiposity
    Guerre-Millo, M
    Gervois, P
    Raspé, E
    Madsen, L
    Poulain, P
    Derudas, B
    Herbert, JM
    Winegar, DA
    Willson, TM
    Fruchart, JC
    Berge, RK
    Staels, B
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (22) : 16638 - 16642
  • [56] THE PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR REGULATES MITOCHONDRIAL FATTY-ACID OXIDATIVE ENZYME GENE-EXPRESSION
    GULICK, T
    CRESCI, S
    CAIRA, T
    MOORE, DD
    KELLY, DP
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (23) : 11012 - 11016
  • [57] Oleoylethanolamide stimulates lipolysis by activating the nuclear receptor peroxisome proliferator-activated receptor α (PPAR-α)
    Guzmán, M
    Lo Verme, J
    Fu, J
    Oveisi, F
    Blázquez, C
    Piomelli, D
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (27) : 27849 - 27854
  • [58] MODULATION OF LIPOPROTEIN PRODUCTION IN HEP G2 CELLS BY FENOFIBRATE AND CLOFIBRATE
    HAHN, SE
    GOLDBERG, DM
    [J]. BIOCHEMICAL PHARMACOLOGY, 1992, 43 (03) : 625 - 633
  • [59] Isozyme-nonselective N-substituted bipiperidylcarboxamide acetyl-CoA carboxylase inhibitors reduce tissue malonyl-CoA concentrations, inhibit fatty acid synthesis, and increase fatty acid oxidation in cultured cells and in experimental animals
    Harwood, HJ
    Petras, SF
    Shelly, LD
    Zaccaro, LM
    Perry, DA
    Makowski, MR
    Hargrove, DM
    Martin, KA
    Tracey, WR
    Chapman, JG
    Magee, WP
    Dalvie, DK
    Soliman, VF
    Martin, WH
    Mularski, CJ
    Eisenbeis, SA
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (39) : 37099 - 37111
  • [60] Activation of gene transcription by prostacyclin analogues is mediated by the peroxisome-proliferators-activated receptor (PPAR)
    Hertz, R
    Berman, I
    Keppler, D
    BarTana, J
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1996, 235 (1-2): : 242 - 247